Absorbable fastener and applying apparatus

ABSTRACT

A surgical fastener apparatus, for securing a surgical mesh material to body tissue including a pair of anchors each having retaining means formed on an outer surface thereof; and a suture tether interconnecting the pair of anchors to one another. The pair of anchors having a substantially cylindrical body having a conically tapered distal end and a planar proximal end. The retaining means includes a series of semi-circular angled projections having a planar proximal surface and a tapered distal end, wherein a center of each of the angled projections is spaced a distance from a longitudinal central axis of the body portion. The surgical fastener is made from a bioabsorbable material which reabsorbs into said body tissue at an appropriate rate, such as for example, polyglycolic acid and polylactic acid.

CROSS REFERENCE TO RELATED APPLICATION

The present application is a Continuation Application claiming thebenefit of and priority to U.S. application Ser. No. 10/399,486, filedon Apr. 16, 2003, which is a U.S. National Stage Application claimingthe benefit of and priority under 35 U.S.C. 371, to InternationalApplication Ser. No. PCT/US01/50165, filed on Oct. 31, 2001, whichclaims the benefit of and priority to U.S. Provisional Application Ser.No. 60/242,647, filed Oct. 23, 2000, the entire contents of each ofwhich is hereby incorporated by reference.

BACKGROUND

1. Technical Field

The present disclosure relates to a surgical fastener and to anapparatus for applying the surgical fastener as well as to a procedurefor fastening objects to body tissue. More particularly, the presentdisclosure relates to an absorbable surgical fastener and apparatus forapplying the absorbable fastener. In addition, the present disclosurerelates to procedures for fastening an object to tissue and toprocedures that require fastening of tissue together.

2. Background of Related Art

Fastening objects to body tissues is a commonly required task in manydifferent surgical applications. One illustrative example of such anapplication is in hernia repair procedures wherein a reinforcingsynthetic mesh material is attached to the tissue. A hernia is a generalterm referring to a protrusion of tissue through a wall of a cavity inwhich the tissue is normally contained, also called rupture. An inguinalhernia is a condition in which a loop of intestine enters the inguinalcanal (i.e., a tubular passage through the lower layers of the abdominalwall). A direct inguinal hernia creates a bulge in the groin area, andan indirect hernia descends into the scrotum. In men, a hernia candevelop at the point where the spermatic cord passes out of the abdomeninto the scrotum. An inguinal hernia is a condition in males whichoccurs in approximately 2% of the male population. Often, an inguinalhernia can be pushed back into the abdominal cavity. However, if theinguinal hernia cannot be forced back through the abdominal wall, theherniated bowel may become trapped in the inguinal ring and/orstrangulated. If the flow of blood is restricted (strangulated hernia)or the intestine is blocked (obstructed), emergency surgery isnecessary. Without treatment, the strangulated loop of intestine dies asa result of a lack of blood to the loop of intestine.

In order to treat the inguinal hernia, surgery is often required toreposition the loop of intestine and secure the weakened muscles in theabdomen. There are two primarily practiced open surgical procedures forhernia repair which procedures use reinforcing synthetic mesh. Oneprocedure is the Lichentstein anterior repair method and the other isthe Stoppa pre-peritoneal repair method. Modifications of theseprocedures exist, as do additional open surgical procedures that do notrequire the placement of reinforcing mesh over the hernia defect.

The Lichtenstein repair method is a “tension-free hemioplasty” based ontwo important facts, namely, inguinal hernias are caused by a metabolicdisorder, which leads to a progressive destruction of thefibroconnective tissue of the groin, making the tissue unsuitable foruse in hernia repair and the fact that traditional tissue repairs areassociated with undue tension at the suture line, which leads to morepostoperative pain, longer recovery time, and a higher rate of.

The Lichtenstein repair method includes the following steps. First, atransverse incision is made within a Langer's line, beginning from thepubic tubercle. The external oblique aponeurosis is opened and thespermatic cord with its cremasteric covering, external spermaticvessels, and the genital nerve are freed from the inguinal floor andlifted with a Penrose drain. The spermatic cord is then dissected freefrom the pubic bone area medial to the pubic tubercle in order to makeroom for extending the mesh beyond the pubic tubercle.

Next, the external oblique aponeurosis is dissected from the underlyinginternal oblique muscle and aponeurosis high enough to make room for aprosthesis. The sac is then dissected from the cord beyond its neck andinverted into the properitoneal space without ligation or excision. Theproximal end is closed, dissected away from the cord structures, andinverted into the preperitoneal space. The medial side of the mesh isthen shaped to the patient's anatomy. The first anchoring suture of themesh fixes the mesh to the anterior rectus sheath where it inserts intothe pubic bone. The lower edge of the mesh is sutured to the inguinalligament using the same suture in a continuous fashion and ends at thelateral border of the internal ring. A slit is next made on the lateralend of the mesh, creating 2 tails. The upper tail is then passed underthe cord and pulled toward the head of the patient, placing thespermatic cord in between the 2 tails. The upper tail is then crossedover the lower one and held with a pair of hemostats. The tails arelater sutured together and tucked under the external obliqueaponeurosis.

The Stoppa method of hernia repair places a single sheet of prostheticmaterial (i.e., surgical mesh) between the peritoneum and themusculopectineal orifice. The surgical mesh is then anchored to Cooper'sligaments using nonabsorbable sutures. The Stoppa hernia repair methodis further described in the attached article in Appendix A, the entirecontents of which are hereby incorporated by reference.

Yet another hernia repair method, known as TransAbdominal PrePeritoneal(TAPP) Laparoscopic Hernia repair method, generally includes thefollowing steps. A pneumoperitoneum is created in the abdomen and anintra-abdominal pressure is maintained. The repair is then initiated. Alaparoscope then inserted and is pointed toward the afflicted inguinalcanal. The peritoneal defect or hernia is identified. A peritonealincision is made, which incision is extended from the lateral aspect ofthe inguinal region to the lateral umbilical ligament. The Cooper'sligament is then exposed as well as the inferior epigastric vessels andthe spermatic Cord. The indirect inguinal hernia sac is then dissectedcarefully from the spermatic cord. A surgical mesh is then inserted intothe intra-abdominal cavity and deployed over the inguinal region. Thereare three methods to place and secure the mesh over the inguinal region.The mesh is then secured in place with a surgical stapler. It is firststapled on to Cooper's ligament followed by placing several staplesperpendicular to the ligament followed by a row more lateral andparallel to Cooper's Ligament. The graft is also anchored around theinferior epigastric vessels and lateral to them. If the mesh is wrappedaround the spermatic cord, both limbs of the mesh are stapled closed.The peritoneum is then closed using additional staples and homeostasisis checked.

Yet another hernia repair method is known as Total ExtraPeritoneal (TEP)Laparoscopic Hernia repair method. This method is identical to the TAPPrepair method, however, it entirely takes place in the preperitonealspace. The TEP method includes the following steps. Unlike the TAPPrepair method, no pneumoperitoneum is created in the TEP repair method.Instead, a small incision is made below the umbilicus (midline) and themidline exposed. An incision is made slightly lateral to the midlineaponevrosis and the anterior and posterior rectus muscle sheaths areexposed. The anatomy must first be clearly identified. Cooper's ligamentshould be first visualized as well as the inferior epigastric vessels.The indirect hernia sac should be bluntly pulled away from the spermaticcord and the inguinal canal. The hernia sac should then be dissected asmedially as possible to allow a surgical mesh to cover the entireinguinal region. The mesh is then inserted and stapled into place as inthe TAPP repair method. With the repair completed the small incisionscan be closed.

The two most common of these methods are the Total ExtraPeritoneal (TEP)repair method and the TransAbdominal PrePeritoneal (TAPP) repair method.As discussed above, each of these methods utilizes a reinforcingsynthetic mesh that must be fixed to the tissue to prevent earlymigration of the mesh away from the hernia site. However, the mesh mustbe anchored into place at first in order to prevent its movement fromthe hernia repair sight. Only after 7-10 days, does the mesh havesufficient tissue in-growth to prevent its motion away from the herniarepair site.

Each of the above disclosed procedures utilizes titanium staples toretain the mesh in place. These staples become permanent residents inthe body cavity A disadvantage of permanent metal staples is thepossibility of the formation of excessive scar tissue (adhesions) whichcan in turn cause further patient complications and hinder futuresurgical procedures. In addition, these permanent staples may beassociated with increased long-term discomfort to the patient as aresult of the hernia repair procedure.

Accordingly, a need exists for an improved surgical fastener andapplying apparatus as well as for methods in securing objects to bodytissue, for example such as in attaching a mesh material for asufficient time to a hernia repair site until sufficient tissuein-growth occurs to retain the mesh in place.

SUMMARY

It is an object of the present disclosure to provide an absorbablesurgical fastener apparatus and methods in which the amount of foreignmaterial in the patients body is reduced, thereby minimizing adhesionformation and reducing fastener-associated long-term discomfort to thepatient.

It is another object of the present disclosure to provide an absorbablesurgical fastener and method which is easier and faster to use thantraditional suturing techniques in open procedures. Further, therelatively high firing force that can be applied to the absorbablefasteners of the present disclosure facilitate more reliable penetrationof tougher tissue materials, such as for example, Cooper's ligament.

It is yet another object of the present disclosure to provide anabsorbable surgical fastener which is radiolucent and provides greaterpeace of mind for the patient.

It is still a further object of the present disclosure to provide anabsorbable surgical fastener apparatus having a suture tether disposedbetween anchoring barbs. The tether provides the advantage of holdingthe mesh in place loosely thus minimizing the tension in the surroundingtissue and reducing fastener pull-out occurrences.

It is another object of the present disclosure to provide a surgicalfastener apparatus which is dimensioned to not penetrate the abdominalwall of the patient and which is provided with a series of barbs havinga relatively larger surface than standard fastener barbs to therebybetter retain the fastener in soft tissue.

The presently disclosed surgical fastener apparatus and method serve thefunction of previously used staples to secure objects to body tissue asperformed in previous methods, for example, mesh being fixed to specificanatomic landmarks surrounding the hernia repair, or attaching mesh totissue, or attaching tissue to tissue or attaching tissue to ligaments.However, the presently disclosed absorbable fastener apparatus andmethod have the uniquely advantageous feature that the absorbablefasteners are utilized to attach the mesh to the tissue for a sufficienttime to allow tissue in-growth to occur on the mesh material. In thismanner, the absorbable fasteners help prevent early mesh migration andthen after sufficient tissue in-growth are absorbed in the body.

A surgical fastener apparatus is provided for securing a surgical meshmaterial to body tissue, in which the apparatus includes a pair ofanchors each having retaining means formed on an outer surface thereofand a suture tether interconnecting said pair of anchors to one another.The fastener apparatus is preferably made from a bioabsorbable materialand is dimensioned such that the apparatus will only be partiallyabsorbed over a period of 2 to 3 weeks after implantation and will becompletely absorbed into the body at any time thereafter.

In an alternate embodiment, the surgical fastener apparatus includes aconical body portion having a pointed distal tip and an enlargedproximal head. The conical body portion being provided with a helicalthread commencing at or near the distal tip and terminating preferablyat a distance spaced from the enlarged proximal head.

In addition, a hernial repair method utilizing the fasteners inaccordance with the present disclosure is provided in which a surgicalmesh is secured in place over the hernia repair site by imbedding thesurgical fasteners in to body tissue through the surgical mesh.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the presently disclosed surgical fastener andmethods will be described herein with reference to the accompanyingdrawing figures wherein:

FIG. 1 is an enlarged perspective view of one embodiment of anabsorbable surgical fastener apparatus constructed in accordance withthe present disclosure;

FIG. 2 is a side view of a barb portion of the absorbable surgicalfastener apparatus of FIG. 1;

FIG. 2A is a side view of a barb portion of an absorbable surgicalfastener apparatus according to an alternate embodiment of the presentdisclosure;

FIG. 3 is an enlarged perspective view of an alternative embodiment ofan absorbable surgical fastener in accordance with the presentdisclosure;

FIG. 4 is an end view of the surgical fastener of FIG. 3;

FIG. 5 is an enlarged perspective view of an absorbable surgicalfastener apparatus including a pair of fasteners as shown in FIG. 3;

FIG. 6 is a cross-sectional view of the absorbable fastener shown inFIG. 5, taken along the longitudinal axis;

FIG. 7 is an illustration of a sequential step in one embodiment ofattaching an object to body tissue using the presently disclosedabsorbable surgical fasteners;

FIG. 8 is a further sequential step according to the method embodimentof FIG. 7;

FIG. 9 is a still further sequential step of the method of FIG. 7;

FIG. 10 is another sequential step of the method of FIG. 7; and

FIG. 11 is another illustration of a step of the method embodiment ofFIG. 7.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

Preferred embodiments of the presently disclosed absorbable surgicalfastener apparatus and method of applying same will now be described indetail with reference to the drawing figures wherein like referencenumerals identify similar or identical structural elements.

The presently disclosed absorbable surgical fastener apparatus andmethod is shown and described herein in connection with open andlaparoscopic inguinal, femoral and ventral hernia repairs. Although notdescribed in detail herein, the absorbable fastener can also be appliedto other procedures which require that objects be attached to bodytissue.

Referring initially to FIGS. 1 and 2, an absorbable surgical fastenerapparatus for connecting objects to body tissue, such as absorbablefastener 10 includes dual fastener anchors 12 and 14 secured to oneanother by a suture tether 16 extending therebetween. Each anchor 12 and14 has a substantially cylindrical body portion 18 having a conicallytapered distal end 20 and a substantially planar proximal end surface22. Anchors 12 and 14 are preferably provided with conically shapeddistal ends 20 for easier penetration of anchors 12 and 14 into hardtissues, such as, for example, Cooper's ligament. While a generallyconical distal end has been disclosed, it is envisioned that othershaped ends (e.g., pyramid, and the like) can be provided. Each anchor12 and 14 is provided with a pair of opposed flattened side surfaces 22extending longitudinally along the length thereof.

Anchors 12 and 14 are provided with barbs 12 a, 12 b, 12 c, and 14 a, 14b, 14 c respectively to inhibit fastener pull-out occurrences in eitherhard or soft tissue. Each barb is semi-circular having a planar proximalsurface 24 which is orthogonal to a central longitudinal axis “A” ofeach anchor 12 and 14, and a tapered lower surface 26. Preferably, barbs12 a-12 c and 14 a-14 c share a common central axis “B”, however, it isenvisioned that each respective barb can have a different center ascompared to other barbs on the anchor. Preferably, central axis “B” isspaced a distance “X” from longitudinal axis “A”. In this manner, thecenter of barbs 12 a-12 c and 14 a-14 c can be positioned to reveal agreater amount of planar proximal surface 24 in order to provide ananchor with predetermined anchoring and securing characteristics forbody tissue without compromising the strength of body portion 18 of eachanchor 12 and 14. For example, if greater retaining strength is desired,distance “X” between central axis “B” and longitudinal axis “A” isincreased thereby forming a bard with a larger planar proximal surface24. In the case of securing a fastener to soft tissue, as is the case inhernia repair, a fastener having a larger projecting barb is desired inorder to better anchor the fastener into the soft tissue of the patient.

While each barb 12 a-12 c and 14 a-14 c is orthogonal to longitudinalaxis “A” of each anchor 12 and 14 respectively, as seen in FIG. 2A, itis envisioned that each barb can be angled relative to longitudinal axis“A” such that barbs 12 a, 12 b and 12 c form a partial thread aroundbody portion 18 of each anchor 12 and 14. In this manner, as each anchor12 and 14 is pressed into body tissue, each anchor 12 and 14 will rotateinto the body tissue.

Although the embodiment of FIGS. 1 and 2 illustrate barbs formedpartially around the circumference of anchors 12 and 14, multiple barbconfigurations can be utilized and are within the scope of the presentdisclosure. For example, in addition to the illustrated configuration,single barb, circumferential barb (i.e., barbs encircling the entireanchor), sharp barbs, dull barbs, multiple barbs, and variousgeometrically shaped barbs may be utilized.

While a planar proximal end 20 has been shown, it is envisioned thateach anchor 12 and 14 can be provided with a notch or detent (not shown)formed in the proximal end thereof. In this manner, when a series ofabsorbable fasteners 10 are joined together, the tapered distal ends 18are received in the detents to thereby maintain the absorbable fasteners10 and anchors 12 and 14 longitudinally aligned with one another.

Absorbable fasteners 10 are preferably made of medical grade absorbablematerials, for example, Polyglycolic Acid (PGA) and Polylactic Acid(PLA). A critical feature of the presently disclosed absorbable fasteneris that the absorbable fastener provide sufficient strength to retain amesh material in place for a desired period of time. For example, in thecase of applying a hernia repair mesh material, it is recommended thatabsorbable fasteners 10 remain in place retaining the mesh material forapproximately 2-3 weeks and be absorbed into the body tissue anytimeafter that.

It is preferred that absorbable fasteners 10 are approximately 3 mmlong, from the tip of distal end 18 to proximal end 20, by approximately1.5 mm in diameter. Other suitably configured and dimensioned fastenersmay also be utilized depending on the particular application. It is alsopreferred that absorbable fasteners 10 are configured and dimensioned toavoid penetrating too far into the tissue. An example of a similarfastener structure and an instrument for applying such fasteners aredisclosed in U.S. Pat. No. 5,997,552 (hereinafter “the '552 patent”),issued to Person et al. and entitled Meniscle Fastener Applying Device,the entire contents of which are hereby incorporated by reference.Unlike the fastener in the '552 patent, the barbs of fastener 10according to the present disclosure have a center “B” which is spaced adistance “X” from the longitudinal axis “A” of the anchor as opposed tothe body of the anchor being cut away to reveal a barb in the '552patent. In this manner, a barb having a larger height is achievedwithout altering the dimensions of the body portion, which larger heightmore firmly secures the anchor of fastener 10 into body tissue ascompared to the fastener disclosed in the '552 patent.

Unlike the applicator instrument for placing absorbable fasteners 10disclosed in U.S. Pat. No. 5,997,552, previously incorporated byreference herein, the applicator according to the present disclosure ispreferably adapted to fire 20 to 30 fasteners per instrument for use ineither open and/or laparoscopic procedures. It is envisioned that theapplicator instrument be either entirely disposable after use or beprovided with a replaceable cartridge of fasteners which can be coupledto the end of a reusable applicator and replaced within a givenprocedure while the handle of such an applicator would still bedisposable but would be reusable within a single procedure. While analternate applier may be used, the fastener applier disclosed in the'552 reference can be used to apply the surgical fasteners disclosedherein.

By way of example, the general procedure of applying a mesh materialduring a hernia repair procedure, is to first create an access to thelocation of the hernia (i.e., incision and dissection) thereby exposingthe hernia; then place a prosthetic mesh over the hernia defect; nextfasten the mesh to the surrounding tissue by firing a plurality ofabsorbable fasteners 10 through the mesh and into tissue to therebysecure the mesh into place; and finally close the access wound.

Turning now to FIGS. 3-5, an alternative embodiment of a surgicalfastener in accordance with the present disclosure in shown generally as200. As seen in FIGS. 3 and 4, fastener 200 includes a substantiallyconical body portion 202 depending from a circular head portion 204.Conical body portion 202 includes a helical thread 206 commencing at apointed distal tip 208 of body portion 202 and terminating at a distancespaced from head portion 204. As the helical thread 206 advances fromdistal tip 206 toward head portion 204, the radial projection of thehelical thread 206 from the body portion 202 increases. While thehelical thread 206 is disclosed as commencing at the distal tip 208, itis envisioned that the helical thread 206 can commence at a distancespaced from the distal tip 208. In addition, head portion 204 can beprovided with a recess or notch (not shown) formed in the center of theproximal surface thereof. The recess being configured to receive thedistal tip 208 of an adjacent fastener 200 therein. In this manner, aseries of fasteners 200 can be aligned in a tip-to-tail fashion with oneanother and share a common axis.

In use, fastener 200 is pressed into body tissue “T”, through surgicalmesh “M”, until the entire body portion 202 of fastener 200 has passedthrough mesh “M” and has been buried in tissue “T”. Head portion 204ensures that fastener 200 does not completely pass through mesh “M”thereby ensuring that mesh “M” is in contact with tissue “T”. Fastener200 includes an arcuate tooth 210 projecting radially outwardly from theproximal end of helical thread 206 and oriented such that the curve ofthe arcuate tooth 210 is oriented to inhibit a rotation of fastener 200which would remove fastener 200 from body tissue “T”.

Turning now to FIG. 5, a surgical fastener apparatus according to thepresent disclosure is shown generally as 300. Similar to fastener 200,surgical fastener apparatus 300 includes a pair of substantially conicalanchors 302 each having a helical thread 304 commencing at a distal tip306 of each anchor 302 and terminating at a proximal end surface 308 ofeach anchor 302. Once again, the radial projection of the helical thread304 on anchor 302 increases as the helical thread 304 advances from thedistal tip 306 to the proximal end of the anchor 302. While the helicalthread 304 is disclosed as commencing the distal tip 306, it isenvisioned that the helical thread 304 can commence at a distance spacedfrom the distal tip 306 just as well. Anchors 302 are connected to oneanother by a suture tether 310 extending therebetween. As seen in FIG.5, the orientation of helical thread 304 on each anchor 302 is in thesame direction. In this manner, as anchors 302 are being imbedded intobody tissue and commence rotating in the direction of helical thread304, suture tether 310 on each anchor 302 will rotate in the samedirection and not become tightened. The proximal end of each helicalthread is provided with an arcuate tooth 312, which arcuate tooth 312 isoriented such that after anchors 302 have been completely imbedded intothe body tissue the tooth 312 will dig into the body tissue if theanchor is rotated in a direction which would remove the anchor from thebody tissue. Similar to fastener 10, surgical fastener apparatus 300 canbe provided with a detent or recess 314 (see FIG. 6) formed in theproximal end surface thereof. In this manner, a series of fasteners 300can be aligned in tip-to-tail fashion with one another in a fastenerapplier so that fasteners 300 share a common axis.

As seen in FIG. 6, helical thread 304 is made up of a distal surface 316and a proximal surface 318 joined together to form a sharp edge 320. Inaddition, suture tether 310 is fixedly retained within anchors 302,however, it is envisioned that suture tether 310 can be rotatablymounted to proximal surface 308.

Fasteners 200 and 300 are also preferably made of medical gradeabsorbable materials, for example, Polyglycolic Acid (PGA) andPolylactic Acid (PLA). A critical feature of the presently disclosedabsorbable fastener is that the absorbable fastener provide sufficientstrength to retain a mesh material in place for a desired period oftime. For example, in the case of applying a hernia repair meshmaterial, it is recommended that absorbable fasteners 200 or 300 remainin place retaining the mesh material for approximately 2-3 weeks and beabsorbed into the body tissue anytime after that. In addition, it ispreferred that absorbable fastener 200 and that each anchor of fastenerapparatus 300 are approximately 3 mm long, from the tip of distal end tothe proximal end, and wherein the proximal end is approximately 1.5 mmin diameter. It is preferred that fastener 200 and fastener apparatus300 are configured and dimensioned to avoid penetrating too far into thebody tissue. Fasteners 200 and 300 can be imbedded into body tissue byeither pressing the fastener in to the tissue and allowing the thread onthe fastener to automatically twist the fastener into the tissue, byproviding a twisting applier which turns the fastener and thus thehelical threads draw the fastener into the body tissue or by acombination of pressing and twisting.

By way of example only, and not to be considered limiting in any way,with reference to FIGS. 7-11, a Lichtenstein repair method will now bedescribed as performed using any of the absorbable surgical fasteners inaccordance with the present disclosure. First, a 5 cm to 6 cm transverseincision is made within a Langer's line, beginning from the pubictubercle. The external oblique aponeurosis (“EOA”) is opened. As shownin FIG. 7, the spermatic cord (“SC”) with its cremasteric covering,external spermatic vessels, and the genital nerve are freed from theinguinal floor and lifted with a Penrose drain. The spermatic cord(“SC”) is dissected free from the pubic bone area for approximately 2 cmmedial to the pubic tubercle in order to make room for extending aprosthetic mesh beyond the pubic tubercle. The external obliqueaponeurosis (“EOA”) is dissected from the underlying internal obliquemuscle and aponeurosis (“IOM”) high enough to make room for a prosthesisthat is 6 cm to 7 cm in height. The sac is then dissected from thespermatic cord (“SC”) beyond its neck and inverted into theproperitoneal space without ligation or excision.

Referring to FIG. 8, a medial side of a mesh (“M”), is shaped to thepatient's anatomy. A first absorbable fastener 10, 200 or 300 is appliedto the mesh to fix the mesh to the anterior rectus sheath where itinserts into the pubic bone. The absorbable fastener 10, 200 or 300 isplaced approximately 2 cm medial to the pubic tubercle in order to besure that the area is covered by the mesh (“M”). Additional absorbablefasteners 10, 200 or 300 are placed therearound and end at the lateralborder of the internal ring. The lower edge of the mesh (“M”) is thenanchored to the inguinal ligament using the same fasteners 10, 200 or300 around the surgical mesh (“M”) and ending at the lateral border ofthe internal ring.

According to one method of the present disclosure, the absorbablefastener 10, 200 or 300 is secured into place by firing the fastenerinto the body tissue such that a first anchor of the surgical fastenerpenetrates through the surgical mesh and into the body tissue and suchthat a second anchor of the surgical fastener is implanted directly intothe body tissue. In this manner, the suture tether 16, 310 (see FIGS. 1,2, 5 and 6) of the fastener apparatus extends partially across thesurgical mesh and partially across body tissue. In an alternativemethod, an absorbable fastener in accordance with the presentdisclosure, can be secured into place such that both anchors areimbedded into the body tissue and pass through the surgical mesh. Iffasteners 200 are used in the method, fasteners 200 are anchored intothe body tissue solely through the mesh.

A slit is then made on the lateral end of the mesh (“M”), as seen inFIG. 9, creating 2 tails—⅔ above (“T1”) and ⅓ below (“T2”). The uppertail (“T1”) is then passed under the cord (“SC”) and pulled toward thehead of the patient, placing the spermatic cord (“SC”) in between the 2tails (“T1, T2”). The upper tail (“T1”) is then crossed over the lowerone (“T2”) and held with a pair of hemostat (“H”), as seen in FIG. 10.The tails (“T1, T2”) are later sutured together and tucked under theexternal oblique aponeurosis, leaving 5 cm to 6 cm of mesh lateral tothe internal ring.

While the upper edge of the mesh is fixed in place, care is taken tokeep the mesh slightly relaxed. This laxity produces a dome-like ripplein the mesh to compensate for increased intra-abdominal pressure whenthe patient stands up from his or her recumbent position during theoperation. If the mesh is kept completely flat, it becomes subject totension when the patient stands up. This pulling effect on the mesh(“M”) and the tissue, is illustrated when the mesh (“M”) is kept flat asshown in FIG. 11. The use of a surgical fastener in accordance with thepresent disclosure effectively eliminates the tension of the surgicalmesh since the anchors of the surgical fastener are relatively movablewith respect to one another. In other words, one anchor is able to movewith respect to the other anchor if needed as the patients body tissueshifts. In so doing, the tension on the mesh is reduced since the suturetether provides the mesh with some room to move since the individualanchors are moveable with respect to one another.

A Total ExtraPeritoneal Laparoscopic Hernia repair using fasteners 10 or300, in accordance with the present disclosure, will now be described.First, a skin incision is created and the fascia is incised. A balloontype distractor is then placed therein and distended in order to createan operative extraperitoneal space. Umbilical trocars and secondarytrocars are then inserted into the extraperitoneal space and the spaceexplored. The medial and lateral structures are then dissected and thespermatic chord identified. A surgical mesh is then cut to the desiredsize and shape such that a slit is provided in order to wrap the mesh oneither side of the spermatic chord. The mesh is then laterally fixed inplace using surgical fasteners 10, 200 or 300 in order to anchor themesh to the tranversus arch and the iliopubic tract. This step isrepeated for the opposite side. The mesh is then medially fixed in placeusing additional fasteners 10, 200 or 300 to the transverses arch and toCooper's ligament or in the alternative, fix the mesh to the medialiliopubic tract. Finally, the incision is closed.

It is envisioned that fasteners 10, 200 or 300 can be used in a TAPPrepair method to replace suturing of the mesh both laterally andmedially. In the TAPP repair method, fasteners 10, 200 or 300 are usedto secure the mesh in to place by penetrating the mesh and beinganchored into the body tissue.

While each of the above described fasteners have been described as beingused in connection with hernial repair surgery, it is envisioned thatfasteners having a similar structure can be used in surgical proceduresfor fastening items to bone or cartilage. In such surgical procedures,the surgical fasteners can be made from surgical grade stainless steel,titanium or any other surgical grade material having sufficient strengthto penetrate bone.

It will be understood that various modifications may be made to theembodiments of the presently disclosed surgical absorbable fastenerapparatus and methods disclosed herein. Therefore, the above descriptionshould not be construed as limiting, but merely as exemplifications ofpreferred embodiments. Those skilled in the art will envision othermodifications within the scope and spirit of the present disclosure.

1. A surgical fastener apparatus for securing a surgical mesh materialto body tissue, comprising: a pair of substantially cylindrical anchorseach defining a longitudinal central axis, wherein each anchor isprovided with a conically tapered distal end and a substantially planarproximal end, and wherein each anchor is further provided with a seriesof semi-circular angled projections having a proximal surface that isangled with respect to the longitudinal axis in such a manner so as todefine a partial thread, a tapered distal end, and defining a commoncentral axis therethrough, wherein the common central axis of saidseries of angled projections, for each anchor, is spaced a distance fromthe longitudinal central axis of said respective anchor; and a flexibletether interconnecting said proximal ends of said pair of anchors toenable freedom of movement of the anchors in multiple directionsrelative to one another.
 2. The surgical fastener according to claim 1,wherein said pair of anchors are made from a bioabsorbable material. 3.The surgical fastener according to claim 2, wherein said bioabsorbablematerial is selected from a material which reabsorbs into said bodytissue at an appropriate rate.
 4. The surgical fastener according toclaim 2, where said bioabsorbable material is selected from the groupconsisting of polyglycolic acid and polylactic acid.
 5. The surgicalfastener according to claim 1, where said pair of anchors and saidtether are dimensioned to be partially absorbed into said body tissuefor at least a period of approximately 2 to 3 weeks immediately afterimplanting and are fully absorbed into said body tissue at any timethereafter.
 6. The surgical fastener according to claim 1, wherein saidpair of anchors have a length of approximately 3 mm from a distal tip ofsaid tapered distal end to said planar proximal end.
 7. The surgicalfastener according to claim 6, wherein said pair of anchors have adiameter of approximately 1.5 mm.
 8. The surgical fastener according toclaim 1, wherein said tether is made from a bioabsorbable material. 9.The surgical fastener according to claim 8, wherein said bioabsorbablematerial is selected from the group consisting of polyglycolic acid andpolylactic acid.
 10. The surgical fastener according to claim 1, whereinsaid tether is nonrigid.
 11. A surgical fastener apparatus, for securinga surgical mesh material to body tissue, comprising: a pair of anchors,each defining a central longitudinal axis, and each having angledprojections formed on an outer surface thereof, wherein the angledprojections for each anchor define a common longitudinal axis which isspaced a radial distance from the central longitudinal axis of therespective anchor, and wherein the angled projections are angled withrespect to the longitudinal axis in such a manner so as to define apartial thread; and a flexible suture tether interconnecting said pairof anchors to one another to enable freedom of movement of the anchorsin multiple directions relative to one another.
 12. The surgicalfastener apparatus according to claim 11, wherein each of said pair ofanchors include a substantially cylindrical body portion having aconically tapered distal end and a substantially planar proximal end.13. The surgical fastener apparatus according to claim 12, wherein saidangled projections include a series of semi-circular angled projectionshaving a substantially planar proximal surface and a tapered distal end,wherein a center of each of said angled projections is spaced a distancefrom a longitudinal central axis of said body portion.
 14. The surgicalfastener apparatus according to claim 13, wherein said suture tether isoperatively coupled to said planar proximal surface of each of said pairof anchors.
 15. The surgical fastener apparatus according to claim 1,wherein each of said pair of anchors includes a conical body portionhaving a helical thread extending therearound.
 16. The surgical fastenerapparatus according to claim 15, wherein said helical thread commencesfrom a distal tip of each of said anchors and terminates at a proximalend of each of said anchors.
 17. The surgical fastener apparatusaccording to claim 16, wherein said suture tether is operatively coupledto said proximal end of each of said anchors.
 18. The surgical fastenerapparatus according to claim 15, wherein said helical thread increasesin a radial direction as said helical thread progresses from said distalend to said proximal end.
 19. The surgical fastener apparatus accordingto claim 11, wherein said pair of anchors are made from a bioabsorbablematerial.
 20. The surgical fastener according to claim 19, wherein saidbioabsorbable material is selected from a material which reabsorbs intosaid body tissue at an appropriate rate.
 21. The surgical fasteneraccording to claim 19, where said bioabsorbable material is selectedfrom the group consisting of polyglycolic acid and polylactic acid. 22.The surgical fastener according to claim 11, where said pair of anchorsand said tether are dimensioned to be partially absorbed into said bodytissue for at least a period of approximately 2 to 3 weeks immediatelyafter implanting and are fully absorbed into said body tissue at anytime thereafter.
 23. The surgical fastener according to claim 11,wherein said pair of anchors have a length of approximately 3 mm from adistal tip of said tapered distal end to said planar proximal end. 24.The surgical fastener according to claim 23, wherein said pair ofanchors have a diameter of approximately 1.5 mm.
 25. The surgicalfastener according to claim 11, wherein said tether is made from abioabsorbable material.
 26. The surgical fastener according to claim 25,wherein said bioabsorbable material is selected from the groupconsisting of polyglycolic acid and polylactic acid.
 27. The surgicalfastener according to claim 11, wherein said suture tether is fixedlysecured to said pair of anchors.
 28. A surgical fastener for securingsurgical mesh material to body tissue, comprising: a conical bodyportion having a pointed distal tip and an enlarged proximal head; and ahelical thread extending radially from said conical body portion,wherein said helical thread commences at said distal tip and terminatesat a distance spaced from said enlarged proximal head.
 29. The surgicalfastener according to claim 28, wherein said helical thread increases ina radial direction as said helical thread progresses from said distalend to said proximal end.
 30. The surgical fastener according to claim29, wherein said fastener is made from a bioabsorbable material.
 31. Thesurgical fastener according to claim 30, wherein said bioabsorbablematerial is selected from the group consisting of polyglycolic acid andpolylactic acid.
 32. The surgical fastener according to claim 29,wherein said fastener is dimensioned to be partially absorbed into saidbody tissue for at least a period of 2 to 3 weeks immediately afterimplanting and is fully absorbed into said body tissue at any timethereafter.
 33. The surgical fastener according to claim 32, whereinsaid fastener has a length of approximately 3 mm from said distal tip tosaid head.
 34. A surgical fastener, comprising: a pair of anchors, eachanchor including: a conical body portion having a pointed distal tip;and a helical thread extending radially from said conical body portion;and a tether interconnecting said pair of anchors to one another. 35.The surgical fastener according to claim 34, wherein said helical threadof each anchor increases in a radial direction as said helical threadprogresses from said distal tip of said conical body portion to aproximal end of said conical body portion.
 36. The surgical fasteneraccording to claim 34, wherein each of said anchors is made from abioabsorbable material.
 37. The surgical fastener according to claim 36,wherein said bioabsorbable material is selected from the groupconsisting of polyglycolic acid and polylactic acid.
 38. The surgicalfastener according to claim 34, wherein said tether is made from abioabsorbable material.
 39. The surgical fastener according to claim 38,wherein said bioabsorbable material is selected from the groupconsisting of polyglycolic acid and polylactic acid.
 40. The surgicalfastener according to claim 38, wherein said tether is nonrigid.
 41. Thesurgical fastener according to claim 34, wherein opposed ends of saidtether are operatively coupled to respective proximal surfaces of eachof said pair of anchors.
 42. The surgical fastener according to claim34, wherein a proximal end of said helical thread of each anchorterminates in a distally oriented tooth.